Syngap1 haploinsufficiency damages a postnatal critical period of pyramidal cell structural maturation linked to cortical circuit assembly (Q35079596)

6 August 2017

title

Syngap1 haploinsufficiency damages a postnatal critical period of pyramidal cell structural maturation linked to cortical circuit assembly (English)

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6 August 2017

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Massimiliano Aceti

1

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Courtney A Miller

9

object named as

Courtney A Miller

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6 August 2017

Thomas K Creson

2

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6 August 2017

Thomas Vaissiere

3

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6 August 2017

Camilo Rojas

4

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6 August 2017

Wen-Chin Huang

5

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6 August 2017

Ya-Xian Wang

6

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6 August 2017

Ronald S Petralia

7

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6 August 2017

Damon T Page

8

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6 August 2017

Gavin Rumbaugh

10

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6 August 2017

language of work or name

English

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publication date

13 August 2014

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6 August 2017

published in

Biological Psychiatry

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6 August 2017

volume

77

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6 August 2017

issue

9

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6 August 2017

page(s)

805-815

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Reduced cognition in Syngap1 mutants is caused by isolated damage within developing forebrain excitatory neurons

6 August 2017

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency

27 September 2018

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27 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326604

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27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326604

Disruption of hippocampus-regulated behavioural and cognitive processes by heterozygous constitutive deletion of SynGAP.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326604

SynGAP regulates steady-state and activity-dependent phosphorylation of cofilin.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326604

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25444158

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures, and severe speech impairment

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25444158

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BIOPSYCH.2014.08.001

1 reference

6 August 2017

1 reference

6 August 2017

1 reference